JPH0340111B2 - - Google Patents
Info
- Publication number
- JPH0340111B2 JPH0340111B2 JP2356483A JP2356483A JPH0340111B2 JP H0340111 B2 JPH0340111 B2 JP H0340111B2 JP 2356483 A JP2356483 A JP 2356483A JP 2356483 A JP2356483 A JP 2356483A JP H0340111 B2 JPH0340111 B2 JP H0340111B2
- Authority
- JP
- Japan
- Prior art keywords
- halon
- aerosol
- fire extinguisher
- container
- present
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- RJCQBQGAPKAMLL-UHFFFAOYSA-N bromotrifluoromethane Chemical compound FC(F)(F)Br RJCQBQGAPKAMLL-UHFFFAOYSA-N 0.000 claims description 8
- 230000007797 corrosion Effects 0.000 claims description 7
- 238000005260 corrosion Methods 0.000 claims description 7
- MEXUFEQDCXZEON-UHFFFAOYSA-N bromochlorodifluoromethane Chemical compound FC(F)(Cl)Br MEXUFEQDCXZEON-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- JLGADZLAECENGR-UHFFFAOYSA-N 1,1-dibromo-1,2,2,2-tetrafluoroethane Chemical compound FC(F)(F)C(F)(Br)Br JLGADZLAECENGR-UHFFFAOYSA-N 0.000 claims description 2
- 229910000831 Steel Inorganic materials 0.000 claims description 2
- 239000010959 steel Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims 1
- 229920004449 Halon® Polymers 0.000 description 20
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 20
- 239000000443 aerosol Substances 0.000 description 18
- 229920000578 graft copolymer Polymers 0.000 description 10
- 239000000843 powder Substances 0.000 description 10
- 229920000247 superabsorbent polymer Polymers 0.000 description 9
- 229920002125 Sokalan® Polymers 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000004584 polyacrylic acid Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- KVBKAPANDHPRDG-UHFFFAOYSA-N dibromotetrafluoroethane Chemical compound FC(F)(Br)C(F)(F)Br KVBKAPANDHPRDG-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 239000004583 superabsorbent polymers (SAPs) Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000003518 caustics Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920001612 Hydroxyethyl starch Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005536 corrosion prevention Methods 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 231100000517 death Toxicity 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical class O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229940050526 hydroxyethylstarch Drugs 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000013842 nitrous oxide Nutrition 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 229920003214 poly(methacrylonitrile) Polymers 0.000 description 1
- -1 polyoxyethylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W90/00—Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
- Y02W90/10—Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics
Description
本願発明は消火剤としてハロンを含有する小型
消火器の容器腐食防止方法に関する。
従来からハロン〔ジブロモテトラフルオロエタ
ン(通称ハロン2402)、ブロモトリフルオロメタ
ン(通称ハロン1301)、ブロモクロロジフルオロ
メタン(通称ハロン1211)〕を使用した消火器は
種々の規格条件が消防法により定められている。
この消防法で定められたところの規格条件を有し
ていない、エアゾール缶型の容器に充填されたハ
ロンは消火器として認められていなかつた。
しかしながら、最近このようなエアゾール缶に
ハロンを充填してなる小型消火器が、家庭内、自
動車、キヤンプなどでの失火の際の初期消火に非
常に有効であることが公的、私的機関で確認され
ており、近く初期消火剤又は器具として認められ
ることになつた。
本願発明者は数年来この種の消火器が初期消火
に有効であることを確認し、その製剤化について
鋭意研究を行つてきた。その中で一番問題となつ
たのは、このハロンを通常のエアゾール缶に充填
したものを長期保存した場合に容器が腐食される
ということであつた。
この原因は、ハロンをエアゾール缶に充填して
消火器を製した場合、微量の水分や空気の存在に
よつてハロンが分解し、腐食性物質を生じて肉厚
の薄いブリキ容器やアルミニウムの如き軽金属容
器は保存中に腐食が起り、万一の場合全く役に立
たないことが判つた。
現在のエアゾール容器は、ブリキ缶で0.21〜
0.3mm、アルミニウム缶で0.21〜0.6mmの肉厚を有
しているが、昨年9月の法改正により、この肉厚
下限規定が撤廃されるに至つた。
必要耐圧を有する範囲内において経済的に最も
有利な方向、即ち、この肉厚は薄くなることは確
実であり、ハロンを充填する場合の腐食は一段と
問題となることは言うまでもない。本発明は上述
のような欠点を改善することを目的として鋭意研
究の結果完成されたものである。
即ち、本発明は肉厚が0.8mm未満である鋼又は
軽金属を使用した、具体的にはブリキ製又はアル
ミニウム製エアゾール容器にハロン2402とハロン
1301、またはハロン1211とハロン1301などが充填
された、いわゆる消火薬剤がハロンであるもの、
もしくは上記の如き消火剤に限らず、ハロンとフ
ロンとの混合物、ハロンと無機消火剤の混合物、
ハロンと無機、有機粉末の混合物、ハロンと圧縮
ガス(炭酸ガス、窒素、笑気ガスなど)の混合
物、この他上述のようなものを二成物または三成
分以上混合した内容物であつて、ハロンを含有す
る場合において発生する容器の腐食防止のため
に、高吸水性ポリマーを容器内に共存させること
で上述のような容器の腐食を防止できることを見
出し、本願発明を完成するに至つた。
この高吸水性ポリマーは自重の数十倍ないし数
百倍の水を保持する能力を有しており、これらに
は、例えば、デンプン−ポリアクリロニトリルグ
ラフト共重合物のケン化物、デンプン−ポリメタ
クリロニトリルグラフト共重合物のケン化物、デ
ンプン−ポリアクリル酸(およびその塩)グラフ
ト共重合物(およびその架橋物)、デンプン−ポ
リアクリル酸エステルグラフト共重合物の加水分
解物、デンプン−ポリメタクリル酸エステルグラ
フト共重合物の加水分解物などがある。そしてデ
ンプンの代わりにヒドロキシエチルデンプン、酸
化デンプンなどのデンプン誘導体、あるいはセル
ロース、メチルセルロース、ヒドロキシエチルセ
ルロース、ヒドロキシプロピルセルロースなどの
セルロース誘導体、あるいは水酸基をもつた多糖
類も使用できる。この他の高吸水性ポリマーとし
てはポリビニールアルコール−ポリアクリル酸グ
ラフト共重合物、ポリアクリル酸架橋物、ポリア
クリル酸自己架橋物、ポリビニールアルコールと
無水マレイン酸との反応物(および塩)、ポリビ
ニールアルコールスルホン酸塩などが挙げられ
る。本願発明に応用できる上記高吸収性ポリマー
のほとんどは球状、破砕状、粉末状、フイルム状
または繊維状などに自由に加工できる性質も兼備
しているため、本願発明におけるエアゾール缶型
の小型消火器内に消火剤と共存させる方法も種々
考えられる。本願発明の目的とするところは、
500g以下の消火薬剤等を充填してなるエアゾー
ル缶型の小型消火器で、ハロンが内容物の一構
成々分であることを必須としたものゝ容器防食で
あるが、消火器の目的とするところは消火であ
り、この目的を損うことは本発明の意図するとこ
ろではない。
消火能力を低下させることなく、防食効果のあ
る形態で添加する必要がある。
例えば、本願発明に用いられる高吸水性ポリマ
ーの粉末状または粒状物を不織布の袋に入れた
り、パルブや放射ボタンの目詰りしない程度、す
なわち微粉末としそのまゝ封入したり、または、
バルブのデイプチユーブに成形して容器内に封入
する方法などがある。
本願発明に利用できる上述のような高吸水性ポ
リマーは化学的な吸水能と保水能を有するが、こ
れらの機能は従来からあるような物理的な吸水、
吸着能を有する無機乾燥剤、例えばシリカゲル、
活性ゼオライトなどとは全く異なるものである。
このように化学的吸水、保水能によつて容器内
の水分増加を抑制し、加えて内容物の構成成分で
あるハロンの分解防止と腐食物質の発生を抑えて
容器の腐食や孔食防止を行うことによつて、万一
の場合の非常時に確実な消火能力を有し、かつ、
我国における年間火災発生件数約60000件、死者
約2000名にものぼる損害の少しでも減少されるこ
とが大きな目的であると共に、この防食方法が社
会的にも経済的にも非常に重要であることを確認
して本発明を完成したものである。
水を含まないエアゾール剤における水分の自然
増加は種々知られているが、ハロンを含むエアゾ
ール缶型の小型消火器においても同様である。こ
の水分は主にバルブ部分を介して容器内に至る場
合がほとんどである。その他、充填される内容物
の水分が多い場合がある。例えば、特開昭57−
75667で示されるようなハロンに無機微粉末を分
散状に存在させる場合において界面活性剤が使用
されるが、界面活性剤の水分含有率は非常に高い
ので、このような剤型においては非常にハロンは
不安定となり腐食が甚しくなる。このような系に
本願発明の高吸水性ポリマーを共存させると非常
に良い結果が得られることも判明している。
本願発明において用いる高吸水性ポリマーのエ
アゾール缶型の小型消火器内への添加量は内容量
に対し0.1%以上あれば効果が認められるが、経
済面、長期の効果面から考えて0.4%〜3%程度
が最も好ましい。
次に本願発明の実施例の一部を示す。
実施例 1
ポリビニールアルコール−ポリアクリル酸グラ
フト共重合体の粉末3gを不織布の袋に入れたも
のと、ハロン2402 392g、ハロン1301 85gをブ
リキ製エアゾール缶に入れて、エアゾール缶型小
型消火器用バルブおよび放射ボタンを装着して
480g入り小型消火器を得た。
実施例 2
デンプン−ポリアクリル酸グラフト共重合物の
破砕粒2gを不織布の袋に入れ、これをバルブの
デイプチユーブに熔着固定し、ハロン1301 50g、
ハロン1211 438gをアルミニウム製エアゾール缶
に入れ、常法によりバルブおよび放射ボタンを装
着して490g入り小型消火器を得た。
実施例 3
デンプン−ポリアクリロニトリルグラフト共重
合物のケン化物の微粉末4g、ハロン2402 320
g、ハロン1301 76gブリキ製エアゾール缶に入
れ、常法により400g入りのエアゾール缶型の小
型消火器を得た。
実施例 4
ハロン1301 40g、ハロン1211 379g、炭酸水
素ナトリウム微粉末25g、ヒドロキシエチルセル
ローズ−ポリメタクリロニトリルグラフト共重合
物のケン化物の微粉末2.5gおよびポリオキシエ
チレンアルキルフエニルエーテル3.5gをアルミ
ニウム製エアゾール容器に入れ常法により450g
入りのエアゾール缶型の小型消火器を得た。
次に本願発明に至つた実験結果の一部を示す。
The present invention relates to a method for preventing corrosion of a container of a small fire extinguisher containing halon as a fire extinguishing agent. Fire extinguishers that use halon (dibromotetrafluoroethane (commonly known as Halon 2402), bromotrifluoromethane (commonly known as Halon 1301), and bromochlorodifluoromethane (commonly known as Halon 1211)) have traditionally been subject to various standards and conditions stipulated by the Fire Service Act. There is.
Halon filled in an aerosol can-type container was not approved as a fire extinguisher, as it did not meet the standards stipulated by the Fire Service Act. However, recently, public and private institutions have discovered that small fire extinguishers made by filling an aerosol can with halon are extremely effective in initially extinguishing a misfire in homes, cars, camps, etc. It has been confirmed that it will soon be recognized as an initial extinguishing agent or device. For several years, the inventor of the present application has confirmed that this type of fire extinguisher is effective for early extinguishing, and has conducted intensive research into its formulation. The biggest problem among them was that if a regular aerosol can filled with halon was stored for a long period of time, the container would corrode. The cause of this is that when a fire extinguisher is made by filling an aerosol can with halon, the halon decomposes in the presence of a small amount of moisture or air, producing corrosive substances that can be used in thin-walled tin containers or aluminum containers. It was found that light metal containers corroded during storage and were completely useless in case of emergency. Current aerosol containers are tin cans with 0.21~
Aluminum cans have a wall thickness of 0.3 mm, and aluminum cans have a wall thickness of 0.21 to 0.6 mm, but due to a legal amendment in September last year, this minimum wall thickness regulation was abolished. It is certain that the wall thickness will be reduced in the economically most advantageous direction within the range that provides the necessary withstand pressure, and it goes without saying that corrosion becomes even more of a problem when filled with halon. The present invention was completed as a result of intensive research aimed at improving the above-mentioned drawbacks. That is, the present invention uses Halon 2402 and Halon in an aerosol container made of steel or light metal with a wall thickness of less than 0.8 mm, specifically made of tin or aluminum.
1301, or those filled with Halon 1211 and Halon 1301, where the so-called extinguishing agent is Halon,
Or not limited to the above extinguishing agents, mixtures of halon and fluorocarbons, mixtures of halon and inorganic extinguishing agents,
A mixture of halon and inorganic or organic powder, a mixture of halon and compressed gas (carbon dioxide, nitrogen, laughing gas, etc.), or a mixture of two or more of the above-mentioned substances, In order to prevent the corrosion of the container that occurs when containing halon, the inventors have discovered that the above-mentioned corrosion of the container can be prevented by coexisting a super absorbent polymer in the container, leading to the completion of the present invention. This super absorbent polymer has the ability to hold water tens to hundreds of times its own weight, and these include, for example, saponified starch-polyacrylonitrile graft copolymers, starch-polymethacrylic Saponified products of nitrile graft copolymers, starch-polyacrylic acid (and its salts) graft copolymers (and crosslinked products), hydrolysates of starch-polyacrylic acid ester graft copolymers, starch-polymethacrylic acid Examples include hydrolyzates of ester graft copolymers. Instead of starch, starch derivatives such as hydroxyethyl starch and oxidized starch, cellulose derivatives such as cellulose, methylcellulose, hydroxyethylcellulose, and hydroxypropylcellulose, or polysaccharides having hydroxyl groups can also be used. Other super absorbent polymers include polyvinyl alcohol-polyacrylic acid graft copolymers, polyacrylic acid crosslinked products, polyacrylic acid self-crosslinked products, reaction products (and salts) of polyvinyl alcohol and maleic anhydride, Examples include polyvinyl alcohol sulfonate. Most of the above-mentioned superabsorbent polymers that can be applied to the present invention also have the property of being freely processable into spherical, crushed, powder, film, or fibrous forms, so that the aerosol can-type small fire extinguisher according to the present invention Various methods can be considered for coexisting with a fire extinguisher. The purpose of the present invention is to
A small aerosol can type fire extinguisher filled with 500g or less of extinguishing agent, etc., which requires halon to be one of the constituents of the contents. Although it is a container corrosion protection, the purpose of the fire extinguisher is However, this is for extinguishing a fire, and it is not the intention of the present invention to undermine this purpose. It must be added in a form that has an anticorrosive effect without reducing fire extinguishing ability. For example, the super absorbent polymer powder or granules used in the present invention may be placed in a non-woven bag, or the powder or granules may be encapsulated as fine powder to the extent that it does not clog the valve or radiation button, or
There is a method of forming the valve into a deep tube and sealing it in a container. The above-mentioned superabsorbent polymer that can be used in the present invention has chemical water absorption and water retention abilities, but these functions are not limited to conventional physical water absorption and water retention.
Inorganic desiccant with adsorption capacity, such as silica gel,
It is completely different from activated zeolite. In this way, chemical water absorption and water retention capabilities suppress the increase in moisture inside the container, and in addition, it prevents corrosion and pitting of the container by preventing the decomposition of halon, which is a component of the contents, and suppressing the generation of corrosive substances. By doing so, we will have reliable fire extinguishing ability in the event of an emergency, and
The major objective is to reduce the damage caused by approximately 60,000 fires and approximately 2,000 deaths each year in our country, as well as the fact that this corrosion prevention method is extremely important both socially and economically. The present invention was completed by confirming the following. Various natural increases in water are known in aerosols that do not contain water, and the same is true for small aerosol can-type fire extinguishers that contain halon. In most cases, this moisture mainly enters the container through the valve part. In addition, there are cases where the contents to be filled have a high moisture content. For example, JP-A-57-
Surfactants are used when inorganic fine powder is dispersed in halon as shown in 75667, but since the water content of surfactants is very high, it is extremely difficult to use in such formulations. Halon becomes unstable and corrodes severely. It has also been found that very good results can be obtained by coexisting the superabsorbent polymer of the present invention in such a system. The amount of super absorbent polymer used in the present invention added to the small aerosol can-type fire extinguisher is effective if it is 0.1% or more based on the content, but from an economical and long-term effect perspective, it should be 0.4% or more. The most preferable amount is about 3%. Next, some embodiments of the present invention will be shown. Example 1 3 g of polyvinyl alcohol-polyacrylic acid graft copolymer powder was placed in a non-woven bag, 392 g of Halon 2402, and 85 g of Halon 1301 were placed in a tin aerosol can to make an aerosol can-shaped small fire extinguisher valve. and equipped with a radiation button.
A small fire extinguisher containing 480g was obtained. Example 2 2 g of crushed grains of starch-polyacrylic acid graft copolymer were placed in a non-woven fabric bag, which was fixed by welding to the deep tube of a valve, and 50 g of Halon 1301,
438 g of Halon 1211 was placed in an aluminum aerosol can, and a valve and emitting button were attached using a conventional method to obtain a small fire extinguisher containing 490 g. Example 3 4 g fine powder of saponified starch-polyacrylonitrile graft copolymer, Halon 2402 320
g, Halon 1301 was placed in a 76g tin aerosol can, and a small aerosol can-type fire extinguisher containing 400g was obtained by a conventional method. Example 4 40 g of Halon 1301, 379 g of Halon 1211, 25 g of fine sodium bicarbonate powder, 2.5 g of fine powder of saponified hydroxyethyl cellulose-polymethacrylonitrile graft copolymer, and 3.5 g of polyoxyethylene alkyl phenyl ether were added to aluminum. 450g by conventional method in a manufactured aerosol container
I got a small aerosol can type fire extinguisher. Next, some of the experimental results that led to the present invention will be shown.
【表】【table】
【表】【table】
【表】
以上の表−、から明らかなように、高吸水
ポリマーの効果は非常に秀れており、0.8mm以下
の肉厚を有するブリキ缶やアルミニウム缶にハロ
ン等を充填してなるエアゾール缶型の小型消火器
の長期安定化に欠かせない物質であるといえる。[Table] As is clear from the above table, the effects of super absorbent polymers are very excellent. It can be said that this substance is essential for the long-term stability of small-sized fire extinguishers.
Claims (1)
使用し、ジブロモテトラフルオロエタン、ブロモ
トリフルオロメタン及びブロモクロロジフルオロ
メタンから選ばれた1種または2種以上を含有す
る消火剤500g以下を充填してなる小型消火器の
容器内に、高吸水性ポリマーを共存させることを
特徴とする小型消火器の容器防食法。1 Made of steel or light metal with a wall thickness of less than 0.8 mm, filled with 500 g or less of a fire extinguishing agent containing one or more selected from dibromotetrafluoroethane, bromotrifluoromethane, and bromochlorodifluoromethane. A method for preventing corrosion of small fire extinguisher containers, which is characterized by coexisting a highly water-absorbing polymer in the container of the small fire extinguisher.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58023564A JPS59150089A (en) | 1983-02-14 | 1983-02-14 | Method for preventing corrosion of container of small- sized fire extinguisher |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58023564A JPS59150089A (en) | 1983-02-14 | 1983-02-14 | Method for preventing corrosion of container of small- sized fire extinguisher |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59150089A JPS59150089A (en) | 1984-08-28 |
JPH0340111B2 true JPH0340111B2 (en) | 1991-06-17 |
Family
ID=12114016
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58023564A Granted JPS59150089A (en) | 1983-02-14 | 1983-02-14 | Method for preventing corrosion of container of small- sized fire extinguisher |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59150089A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61195979A (en) * | 1985-02-25 | 1986-08-30 | Kao Corp | Rust preventive material for metal |
JPS61195980A (en) * | 1985-02-25 | 1986-08-30 | Kao Corp | Material for rust prevention of metal |
US9463341B2 (en) * | 2011-10-25 | 2016-10-11 | Kidde Technologies, Inc. | N2/CO2 fire extinguishing system propellant gas mixture |
CN113335733B (en) * | 2021-08-05 | 2021-10-29 | 南通语森家纺科技有限公司 | Case is deposited to fabrics |
-
1983
- 1983-02-14 JP JP58023564A patent/JPS59150089A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59150089A (en) | 1984-08-28 |
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